Canonical Allele Identifier: PA645485536
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 430318
ClinVar RCV Id: RCV000493627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Ile178Asn
CA384926191
NM_005555.4:c.533T>A